Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_assertion description "[Here, we show that constitutive loss of Asxl1 results in developmental abnormalities, including anophthalmia, microcephaly, cleft palates, and mandibular malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_assertion evidence source_evidence_literature NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_assertion SIO_000772 24218140 NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_assertion wasDerivedFrom befree-20150227 NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_assertion wasGeneratedBy ECO_0000203 NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978413.RAiMfFNsjR1MMqihJks91J98_BdvhR1L-CAo1T09LS3es130_provenance.